Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1260326
rs1260326
GCKR
81 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.800 1.000 23 2008 2019
dbSNP: rs964184
rs964184
ZPR1
47 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.800 1.000 22 2009 2019
dbSNP: rs12678919
rs12678919 		10 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 0.800 1.000 13 2009 2019
dbSNP: rs2954029
rs2954029 		14 0.807 0.160 8 125478730 intron variant A/T snv 0.42 0.800 1.000 13 2009 2019
dbSNP: rs780094
rs780094
GCKR
62 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.800 1.000 10 2007 2019
dbSNP: rs10401969
rs10401969
SUGP1
25 0.776 0.240 19 19296909 intron variant T/C snv 0.10 0.800 1.000 9 2010 2019
dbSNP: rs17145738
rs17145738
TBL2
11 0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11 0.800 1.000 9 2008 2019
dbSNP: rs651821
rs651821
APOA5
17 0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 0.800 1.000 9 2012 2019
dbSNP: rs328
rs328
LPL
19 0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 0.800 1.000 8 2007 2019
dbSNP: rs439401
rs439401 		8 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 0.800 1.000 8 2009 2019
dbSNP: rs662799
rs662799
APOA5
33 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.800 1.000 8 2012 2019
dbSNP: rs174546
rs174546
FADS1 ; FADS2
17 0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 0.800 1.000 7 2008 2019
dbSNP: rs4846914
rs4846914
GALNT2
6 0.925 0.080 1 230159944 intron variant G/A snv 0.45 0.800 1.000 7 2008 2019
dbSNP: rs10096633
rs10096633 		8 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 0.800 1.000 6 2009 2019
dbSNP: rs1042034
rs1042034
APOB
15 0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 0.800 1.000 6 2010 2019
dbSNP: rs10503669
rs10503669 		8 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 0.800 1.000 6 2008 2019
dbSNP: rs12721054
rs12721054
APOC1
3 19 44919330 3 prime UTR variant A/G snv 3.7E-02 0.800 1.000 6 2012 2019
dbSNP: rs17482753
rs17482753 		8 1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02 0.800 1.000 6 2007 2019
dbSNP: rs1800588
rs1800588
LIPC ; ALDH1A2
16 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.800 1.000 6 2012 2019
dbSNP: rs2068888
rs2068888 		5 10 93079885 downstream gene variant G/A snv 0.42 0.800 1.000 6 2010 2019
dbSNP: rs3764261
rs3764261 		26 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 0.800 1.000 6 2009 2018
dbSNP: rs780093
rs780093
GCKR
30 0.763 0.240 2 27519736 intron variant T/C snv 0.68 0.800 1.000 6 2011 2019
dbSNP: rs2075290
rs2075290
ZPR1
10 0.882 0.160 11 116782580 intron variant C/G;T snv 0.800 1.000 5 2011 2019
dbSNP: rs2131925
rs2131925
DOCK7
6 1 62560271 intron variant G/T snv 0.57 0.800 1.000 5 2010 2019
dbSNP: rs28927680
rs28927680
BUD13
4 11 116748357 3 prime UTR variant C/G;T snv 0.800 1.000 5 2008 2019